Zhang L, Wu W T
School of Lifesciences and Biotechnology, China Pharmaceutical University, Nanjing 215009, PR China.
Nat Prod Res. 2008 Apr 15;22(6):554-63. doi: 10.1080/14786410701592679.
The characterization of an L-amino acid oxidase purified from Agkistrodon acutus snake venom was investigated. An L-amino acid oxidase (LAAO) was purified from A. acutus snake venom through DEAE Sepharose F.F. and Source 30 S chromatography. The molecular mass of this enzyme was determined by SDS-PAGE, size exclusion chromatography, and mass spectrometry. Substrate specificity, cytotoxicity, antitumor activity in vivo, and apoptosis-inducing activity were assayed. The LAAO purified from A. acutus snake venom was designated as ACTX-6. It is a covalently bound homodimer and its molecular mass is about 96 kDa. This enzyme preferred to oxidize hydrophobic L-amino acids; the best substrates were L-Met, L-Leu, L-Trp, and L-Phe. ACTX-6 demonstrated cytotoxicity in vitro and could inhibit tumor growth in vivo. Flow cytometry analysis showed that it could markedly increase accumulation of sub-G1 phase, which suggested that this enzyme could induce apoptosis. ACTX-6 could effectively inhibit tumor growth and it is a potential substance to develop into an antitumor drug.
对从尖吻蝮蛇毒中纯化的L-氨基酸氧化酶进行了特性研究。通过DEAE Sepharose F.F.和Source 30 S色谱法从尖吻蝮蛇毒中纯化出一种L-氨基酸氧化酶(LAAO)。通过SDS-PAGE、尺寸排阻色谱法和质谱法测定了该酶的分子量。测定了底物特异性、细胞毒性、体内抗肿瘤活性和诱导凋亡活性。从尖吻蝮蛇毒中纯化的LAAO被命名为ACTX-6。它是一种共价结合的同二聚体,分子量约为96 kDa。该酶优先氧化疏水性L-氨基酸;最佳底物为L-蛋氨酸、L-亮氨酸、L-色氨酸和L-苯丙氨酸。ACTX-6在体外表现出细胞毒性,并且能够在体内抑制肿瘤生长。流式细胞术分析表明,它可显著增加亚G1期的积累,这表明该酶可诱导凋亡。ACTX-6能够有效抑制肿瘤生长,是一种有潜力开发成抗肿瘤药物的物质。